Canonical Allele Identifier: CA1806376452

Gene: GRHL2

Linked Data

• dbSNP Id: rs1811196972

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543462_101543466del , CM000670.2:g.101543462_101543466del	GRCh38
NC_000008.10:g.102555690_102555694del , CM000670.1:g.102555690_102555694del	GRCh37
NC_000008.9:g.102624866_102624870del	NCBI36
NG_011971.1:g.56023_56027del
NG_011971.2:g.56023_56027del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.216+26_216+30del MANE Select	ENSP00000495564.1:n.216+26_216+30del
ENST00000251808.7:c.216+26_216+30del	ENSP00000251808.3:n.216+26_216+30del
ENST00000395927.1:c.168+26_168+30del	ENSP00000379260.1:n.168+26_168+30del
ENST00000472106.2:n.570_574del
NM_024915.3:c.216+26_216+30del	NP_079191.2:n.216+26_216+30del
XM_011517305.1:c.168+26_168+30del	XP_011515607.1:n.168+26_168+30del
XM_011517306.1:c.168+26_168+30del	XP_011515608.1:n.168+26_168+30del
XM_011517307.1:c.216+26_216+30del	XP_011515609.1:n.216+26_216+30del
NM_001330593.1:c.168+26_168+30del	NP_001317522.1:n.168+26_168+30del
XM_011517306.3:c.168+26_168+30del	XP_011515608.1:n.168+26_168+30del
XM_011517307.3:c.216+26_216+30del	XP_011515609.1:n.216+26_216+30del
NM_001330593.2:c.168+26_168+30del	NP_001317522.1:n.168+26_168+30del
NM_024915.4:c.216+26_216+30del MANE Select	NP_079191.2:n.216+26_216+30del